Big Benefits, Scalable Price: The SAS® Cloud-Based Clinical Platform for SMBs
Learn how small-to-midsize pharmas, biotechs, medical device manufacturers and CROs can benefit from a compliant cloud-based solution to facilitate clinical trials.
March 10 • 10 a.m. ET • Cost: Complimentary
About the webinar
Collecting, managing, standardizing and analyzing clinical trial data is crucial in the clinical submission process for regulatory approval for new medical or biotech devices.
SAS has a scalable solution to help small-to-midsize organizations with the clinical trial process.
We’ll demo the SAS Life Science Analytics Framework and show how it can benefit small-to-midsize organizations (pharma, biotech, medical device and CRO).
What you'll learn:
- How the SAS framework can help define and manage policies to ensure FDA compliance.
- How to easily drive collaboration and workflow between preclinical, biostatistics, operations and medical affairs.
- How you can end the struggle with the management and implementation of clinical data standards (CDASH, SDTM, SEND, ADaM and Define-XML).
- How you can quickly answer regulatory inquiries and trace data pedigree back to the source.